A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518109



Internal ID15445402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14286352..14325619hg38UCSC Ensembl
InnerchrX:14304474..14343741hg19UCSC Ensembl
InnerchrX:14214395..14253662hg18UCSC Ensembl
InnerchrX:14064131..14103398hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3839268
hg1939268
hg1839268
hg1739268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694202
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518109
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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